Segmented intravaginal ring for the combination delivery of hydroxychloroquine and anti-CCR5 siRNA nanoparticles as a potential strategy for preventing HIV infection

• Published in: Drug delivery and translational research Vol. 12; no. 4; pp. 816 - 825
• Main Authors: Traore, Yannick L., Chen, Yufei, Padilla, Fernanda, Ho, Emmanuel A.
• Format: Journal Article
• Language: English
• Published: New York Springer US 01-04-2022
• Subjects: Administration, Intravaginal; Biomedical and Life Sciences; Biomedicine; Female; HIV Infections - drug therapy; HIV Infections - prevention & control; Humans; Hydroxychloroquine; Nanoparticles; Original; Original Article; Pharmaceutical Sciences/Technology; RNA, Small Interfering; Anti-CCR5 siRNA; HIV; pH-responsive polymer; Intravaginal ring; Solid lipid nanoparticles
• ISSN: 2190-393X; 2190-3948
• DOI: 10.1007/s13346-021-00983-w

 
Vaginal drug delivery has been shown to be a promising strategy for the prevention of sexually transmitted infections. Therapy delivered at the site of infection has many advantages including improved therapeutic efficacy, reduction in systemic toxicity, and reduced potential for development of drug resistance. We developed a “smart” combination intravaginal ring (IVR) that will (1) provide continuous release of hydroxychloroquine (HCQ) to induce T cell immune quiescence as the first-line of defense and (2) release nanoparticles containing anti-CCR5 siRNA only during sexual intercourse when triggered by the presence of seminal fluid as the second-line of defense. The IVR was capable of releasing HCQ over 25 days with a mean daily release of 31.17 ± 3.06 µg/mL. In the presence of vaginal fluid simulant plus seminal fluid simulant, over 12 × more nanoparticles (5.12 ± 0.9 mg) were released over a 4-h period in comparison to IVR segments that were incubated in the presence of vaginal fluid simulant alone (0.42 ± 0.19 mg). Anti-CCR5 siRNA nanoparticles were able to knockdown 83 ± 5.1% of CCR5 gene expression in vitro in the CD4
+
T cell line Sup-T1. The IVR system also demonstrated to be non-cytotoxic to VK2/E6E7 vaginal epithelial cells.
Graphical abstract